Invictus 17100-18-2Recalls & reported problems
Alphatec Spine, Inc. · BLUNT TIP NITINOL GUIDEWIRE 18" · Class 1
All models of Invictus (96)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00190376220253), received between Apr 29, 2026 and Apr 29, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
- Material Separation2
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 29, 2026Break; Material Separation
IT WAS REPORTED THAT TWO GUIDEWIRE TIPS BROKE OFF PAST THE SCREW AND REMAIN IN THE PATIENT. THIS IS REPORT 2 OF 2.
Patient problems: Foreign Body In Patient
MAUDE report 25032636 ↗InjuryApr 29, 2026Break; Material Separation
IT WAS REPORTED THAT TWO GUIDEWIRE TIPS BROKE OFF PAST THE SCREW AND REMAIN IN THE PATIENT. THIS IS REPORT 1 OF 2.
Patient problems: Foreign Body In Patient
MAUDE report 25032512 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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